| Tag | Content |
|---|
EnhancerAtlas ID | HS052-00131 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:8013690-8014770 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK4 | MA0076.2 | chr1:8014349-8014360 | GCCGGAAGTGG | - | 6.62 | | Gabpa | MA0062.2 | chr1:8014350-8014361 | CCGGAAGTGGA | + | 6.32 | | ZBTB7A | MA0750.2 | chr1:8014348-8014361 | CGCCGGAAGTGGA | + | 6.11 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCCAAGGCG GGAGGATCGC TTGAGCCCAG GGGTTCAATA TAAGCCTTGG CAACATAGCA 60
AGACCCCGTC TCTACTTCTC AGAAAGAAAA CAAAAGAAAT AAGATGCCAT GGAAGGGATG 120
GCAATAAGCG TTTTCCATAA ACAACCCGAG AGAGAGAAAC AGAAAACGCT GTCCAAGCTA 180
AGCCTTGCTT CCACACTGGG CTTTGCAGAT TTTCCAATGA GCCACCAACG AGGTGGTTAA 240
AACATCAGAG ACTGCATCCG ATTCCCCAAG ACACCAAGGC TCTCGGGATG GGAACAGGCA 300
AATCGTCGTC GTTCTTTGCT GAGCCTGCGG GCTGCGGTCA CCAGAACGAA TCTGGGCCCA 360
GCAGGTGCCA AGGGCTCGAC CTCCCGCCTT GCATCCGGCA GGCCGCACAC ACCCCTCGGA 420
AGTCGGCGAG ATCGCTGAGG CAAAGCGACT CCAGGGCGCA GAGACCCACA CGCGACGCTC 480
TAAAGGAAGT GACCTTTAGG GGCTGTTACT CTCAGACCAG GCCCAGCAGC ACCCGGCGCA 540
TTTACGTCGG ATCTGACCCC TGCAAGCACC GGCGCGACCG CGCTAGCGGC TGGGAACACG 600
CGACGGTCCC GCCCACTGCG ACCTGACTCG GCCAATCCCG GGTGGCGCAT GCTGCGGCCG 660
CCGGAAGTGG ACCTACGTCA TGCAGGTCAG TCGGTAGGTT TCCGGCGCCC AGCGCCCCGT 720
GGGAGTTGTG TCTGGTGGCC CACGCTGGGG GGGGGCTCTT CACACTGGTG GGCGCAGAGG 780
CGAAGCCGTT CCCAGGGCCC CTCACAGAAC TCGGTGTCAG AATTTCCCCC CTTGCACCAG 840
CGCCGCCTCA AATGTCAGGG CTCGCCCACT CTTCTCCGGT CTCGCCGACA TAACCTTTTG 900
GGGGCTCCAG AGGGGAAATT TGCCGTTTCT GCCGGACCGC TCTAGAGCGT GCCTGAACCC 960
GGCCTTTATG GGATGTTGAC AGCTACGTTT ATTCAGTGCC CCAGAGGCCT TCTTTATGCC 1020
CAGTAACTAC AATTTAAATT CCTTCTCTGC TTCATTTTGT AGTCGTCTGG TGAATTTGAC 1080
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